Know if it’s recalled — and exactly what to do.

B. Braun Medical Inc recalls 0.9% Sodium Chloride Injection USP, E8000, 1000mL container, Rx only, B. Braun Medical Inc., Irvine, CA, NDC

B. Braun Medical recalls 1000mL 0.9% Sodium Chloride Injection (Rx only) with lot numbers J2L763/J2L764, expiring March 2025, due to possible particulate matter. Consumers should contact the company for details.

INDIAN CHALLENGER DARK HORSE (2024) recall — Suspension

Karl Storz Endoscopy recalls Karl Storz - Endoskope , REF: 27830KA, Nephroscope for MIP M, Rx only, CE 0123

Karl Storz recalls nephrosopes with unapproved reprocessing methods that may not be safe for medical use. Affected units have specific serial numbers.

Karl Storz Endoscopy recalls Karl Storz - Endoskope , REF: 27840KA, Nephroscope for MIP L, Rx only, CE 0123

Karl Storz recalls nephrosopes with unapproved reprocessing methods that may not be safe for medical use. Affected models include REF: 27840KA, CE 0123.

Karl Storz Endoscopy recalls Karl Storz - Endoskope , REF: 27293AA, Hopkins Telescope 6, Rx only, CE 0123

Karl Storz recalls endoscopy devices with unapproved reprocessing methods that may not meet FDA safety standards. Affected products include specific models sold under CE 0123 certification.

Karl Storz Endoscopy recalls Karl Storz - Endoskope , REF: 27295AA, Hopkins Telescope 6, 18 Fr, Rx only, CE 0123

Karl Storz recalls specific endoscopy devices due to unapproved reprocessing methods that may not meet FDA safety standards. Affected devices include Hopkins Telescope 6 models with certain serial numbers.

Karl Storz Endoscopy recalls Karl Storz - Endoskope , REF: 27294AA, Hopkins Telescope 6, 18 Fr, Rx only, CE 0123

Karl Storz recalls endoscopy devices with unapproved reprocessing methods. FDA requires safety review before use. Affected devices include specific models and lots.

Karl Storz Endoscopy recalls Karl Storz - Endoskope , REF: 27093AA Hopkins Telescope 6, Rx only, CE 0123

Karl Storz recalls Endoskope Telescope 6 devices with unapproved reprocessing methods. FDA requires safety review before use to prevent risks.

Karl Storz Endoscopy recalls Karl Storz - Endoskope , REF: 27092AMA, Hopkins Telescope 6, Rx only, CE 0123

Karl Storz recalls endoscopy devices with unapproved reprocessing methods. FDA requires safety review before use. Affected devices include specific models and lots.

Glenmark Pharmaceuticals Inc., USA recalls Glenmark, Azelaic Acid Gel, 15 %, 50 grams, Rx only, Manufactured by: Glenmark Pharmaceuticals Limited, Colvale-Bardez,

Glenmark Pharmaceuticals recalls 15% azelaic acid gel (50g, Rx only) due to CGMP deviations. Affected lots manufactured in India for US sale. No specific remedy stated in recall notice.

Frozen Food Processors, Inc. recalls Frozen Food Processors - Regular Cornbread Muffins packaged in 2oz corrugated cardboard boxes lined with food grade

Frozen Food Processors recalls regular cornbread muffins made without state license in unsanitary conditions. Products packaged in 2oz cardboard boxes with food-grade plastic. Affected batches include FFP 15600+ with specific lot numbers and best by dates.